Literature DB >> 6172467

Endocytic vesicles and surface invaginations in cultured vascular endothelium: a morphometric comparison.

P F Davies, L Kuczera.   

Abstract

Ruthenium red staining of plasma membrane glycoproteins of confluent cultured arterial endothelial cells revealed that the limiting membrane of many apparently discrete cytoplasmic vesicles was continuous with the plasmalemma. Surface invaginations accessible to ruthenium red appeared as vesicles when sectioned out of the plane of attachment to the cell surface, Morphometric analysis of ruthenium red-positive (RR+) and ruthenium red-negative vesicles (RR-) indicated that 47.2% of the total apparent vesicle population was RR+ and that those infoldings accounted for 19.6 +/- 1.4% of the cell surface in transverse sections. Whereas 14.9% of the true vesicles (ruthenium red-negative) were coated vesicles, only 1.1% of RR+ "vesicles" were coated pits. These studies show that although many deep infoldings of the cell surface may be misinterpreted as vesicles, almost all are uncoated. The existence of discrete coated vesicles (independent of coated pits) in vascular endothelium in vitro is readily apparent.

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Year:  1981        PMID: 6172467     DOI: 10.1177/29.12.6172467

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  3 in total

1.  Distribution of endothelial vesicles in the microvasculature of skeletal muscle and brain cortex of the rat, as demonstrated by tannic acid tracer analysis.

Authors:  Y Noguchi; T Yamamoto; Y Shibata
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

2.  Diffusion-limited forward rate constants in two dimensions. Application to the trapping of cell surface receptors by coated pits.

Authors:  B Goldstein; R Griego; C Wofsy
Journal:  Biophys J       Date:  1984-11       Impact factor: 4.033

3.  Plasmalemmal proteins of cultured vascular endothelial cells exhibit apical-basal polarity: analysis by surface-selective iodination.

Authors:  W A Muller; M A Gimbrone
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

  3 in total

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